rs886037779, PEX6

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
HEIMLER SYNDROME 2
CUI: C4225267
Disease: HEIMLER SYNDROME 2
12 1.000 6 42978497 missense variant G/C snv 4.0E-06 0.800 1.000 3 2009 2016